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Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
Authors:Ciszek-Lenda  Marta  Strus  Magdalena  Walczewska  Maria  Majka  Grzegorz  Machul-Żwirbla  Agnieszka  Mikołajczyk  Diana  Górska  Sabina  Gamian  Andrzej  Chain  Benjamin  Marcinkiewicz  Janusz
Affiliation:1.Chair of Immunology, Jagiellonian University Medical College, Kraków, Poland
;2.Chair of Microbiology, Jagiellonian University Medical College, Kraków, Poland
;3.Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroc?aw, Poland
;4.Division of Infection and Immunity, UCL, London, UK
;
Abstract:Objective

Pseudomonas aeruginosa effectively facilitate resistance to phagocyte killing by biofilm formation. However, the cross talk between biofilm components and phagocytes is still unclear. We hypothesize that a biofilm provides a concentrated extracellular source of LPS, DNA and exopolysaccharides (EPS), which polarize neighbouring phagocytes into an adverse hyperinflammatory state of activation.

Methods

We measured the release of a panel of mediators produced in vitro by murine neutrophils and macrophages exposed to various biofilm components of P. aeruginosa cultures.

Results

We found that conditioned media from a high biofilm-producing strain of P. aeruginosa, PAR5, accumulated high concentrations of extracellular bacterial LPS, DNA and EPS by 72 h. These conditioned media induced phagocytes to release a hyperinflammatory pattern of mediators, with enhanced levels of TNF-α, IL-6, IL12p40, PGE2 and NO. Moreover, the phagocytes also upregulated COX-2 and iNOS with no influence on the expression of arginase-1.

Conclusions

Phagocytes exposed to biofilm microenvironment, called by us biofilm-associated neutrophils/macrophages (BANs/BAMs), display secretory properties similar to that of N1/M1-type phagocytes. These results suggest that in vivo high concentrations of LPS and DNA, trapped in biofilm by EPS, might convert infiltrating phagocytes into cells responsible for tissue injury without direct contact with bacteria and phagocytosis.

Keywords:
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